Benazepril Hydrochloride
- Product NDC
- 68071-5130
- 11-digit product format
- 680715130
- Labeler code
- 68071
- Product ID
- 68071-5130_1b54a8a1-0ece-633c-e063-6394a90a1be2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N1SN99T69T | BENAZEPRIL HYDROCHLORIDE | 86541-74-4 | BENAZEPRIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-5130-0 | 68071513000 | 100 TABLET, COATED in 1 BOTTLE (68071-5130-0) | 2019-12-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Benazepril Hydrochloride | NuCare Pharmaceuticals,Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL | 3 |